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ACTIVE NOT RECRUITING
NCT03057730
PHASE4

A Clinical Trial Testing Root Coverage With Acellular Dermal Matrix in Thin and Thick Gingival Biotypes

Sponsor: Tufts University

View on ClinicalTrials.gov

Summary

Gingival recession is a common defect among the American population. It is also a major cause for root decay, hypersensitivity, contributes to tooth mobility and low self-esteem. Acellular dermal matrix, a human-derived grafting material has been put on the market for the treatment of gingival recession. Treating gingival recession with this material has been a validated treatment option for years. However, treatment outcomes in two patient populations, namely those with thin biotypes and those with thick biotypes, has not been investigated. This study will observe the primary treatment outcomes in the two patient groups at 5 time points - 3 months, 6 months and 12 months post-surgery to observe short term outcomes; additional 24 months and 48 months post-surgery to observe long term outcomes.

Official title: Acellular Dermal Matrix Combined With Coronally Advanced Flap in the Treatment of Multiple Recession Defects in Thin Versus Thick Periodontal Biotype Population: A Controlled Clinical Investigation

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

34

Start Date

2015-08

Completion Date

2025-09

Last Updated

2024-08-20

Healthy Volunteers

Yes

Interventions

BIOLOGICAL

Acellular Dermal Matrix

ADM is a human-derived allograft material, treated to remove all cellular components so that only the connective tissue matrix remains.

Locations (1)

Tufts University School of Dental Medicine

Boston, Massachusetts, United States